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Which is an autosomal chromosomal mutational disorder?

Important Questions on Heredity and Variation

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Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorder in Human
A human female with Turner's syndrome
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Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorder in Human

The following family tree traces the occurrence of a rare genetic disease. The filled symbols signify the individuals with the disease, whereas the open symbols signify healthy individuals.

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Based on this information, the disease is most likely to be:

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Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorder in Human
Choose the odd one and write it:
Dwarfism, Goiter, Thalassaemia, Diabetes Mellitus
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Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorder in Human

Choose the correct option for the pedigree analysis given below:

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Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorder in Human
The genetic disorder in which an individual has an overall masculine development, gynaecomastia and is sterile:
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Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorder in Human
Which of the following muscular disorders is inherited?
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Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorder in Human
Give one example of autosomal genetic disease. What is its reason?
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Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorder in Human
Name the human disease due to autosomal dominant gene :
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Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorder in Human
A disease caused by an autosomal primary non-disjunction is
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Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorder in Human
Which of the following occurs due to the presence of autosome linked dominant trait?
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Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorder in Human
A disease which causes the black color of the urine
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Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorder in Human
In humans, attached earlobes are a dominant feature over free earlobes while hypertrichosis of the ear is a holandric (Y-linked) feature. A man with attached earlobes and extensive hair on pinna married a woman having free earlobes. The couple had one son with attached earlobes and hairy pinna, another son with free earlobes and hairy pinna and two daughters with attached earlobes. One of the daughters married a man with free earlobes and sparse hair on pinna. They had two sons. What would be the characteristics of their pinnae? What would be characteristic of their two daughters?
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Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorder in Human
Find out the MISMATCHED pair.
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Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorder in Human
In humans, attached earlobes are a dominant feature over free earlobes while hypertrichosis of the ear is a holandric (Y-linked) feature. A man with attached earlobes and extensive hair on pinna married a woman having free earlobes. The couple had one son with attached earlobes and hairy pinna, another son with free earlobes and hairy pinna and two daughters with attached earlobes. One of the daughters married a man with free earlobes and sparse hair on pinna. They had two sons. What would be the characteristics of their pinnae?
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Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorder in Human
Both Down's syndrome and Turner's syndrome are examples of chromosomal disorders. Cite the differences between the two.
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Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorder in Human
Edward syndrome occurs due to abnormalities in sex chromosoms.
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Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorder in Human
Which of the following is a correct match?
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Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorder in Human
Turner's syndrome in humans is caused by:
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Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorder in Human
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On the basis of above pedigree chart, select the correct option
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Biology>Genetics and Evolution>Heredity and Variation>Mendelian Disorder in Human
A parent has the autosomal dominant disease then what will be the probability of diseased offspring (irrespective of the sex of the child) :